Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

-/A | MAF: 0.12 (A)

Chromosome 7: between 151573142 and 151573143 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs146040967, rs374204532

This variation has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 1092 individual genotypes.

Variation displays